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Shaping Care Home COVID-19 Testing Policy (VIVALDI-CT)

Primary Purpose

COVID-19

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Lateral Flow Device
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for COVID-19 focused on measuring Lateral Flow Device

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Only care home staff are eligible to participate in the testing intervention. This includes temporary (agency) staff with no restrictions i.e. catering staff, administrative staff, maintenance staff, in addition to those in a resident-facing role. All care home staff, residents, visitors and relatives are eligible to participate in interviews undertaken as part of the process evaluation. All care home residents at participating home are eligible for data collection and analysis of the outcomes specified. Exclusion Criteria: Visitors, residents and relatives are not eligible to take part in the testing intervention. Staff who visit the care home to provide care but are not employed by the care home e.g. GPs, health visitors are not eligible to take part in either the interviews or the testing intervention.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    No Intervention

    Arm Label

    Arm A

    Arm B

    Arm Description

    LFD testing for Covid-19 with sickness support payment. Care providers will receive funding to reimburse the costs of employing agency staff to cover sickness absence in asymptomatic staff who test positive for COVID.

    Usual Care

    Outcomes

    Primary Outcome Measures

    Primary Outcome
    The primary outcome is the incidence of COVID-19 related hospital admissions in residents, defined as admissions with a relevant ICD-10 codes (COVID hospitalisations to be defined as any hospital admission record with a primary or secondary ICD10 code of 'U071') and/or admissions in residents who test positive for COVID-19 within 24h following admission or in the 7 days before hospital admission. This has been selected because it is the most important outcome for policymakers.

    Secondary Outcome Measures

    Incidence rate of hospital admissions
    Incidence rate of hospital admissions (all-cause) in residents for non-elective care, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Incidence rate of COVID-associated mortality in residents
    Incidence rate of COVID-associated mortality in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial. COVID-associated mortality will be defined as death within 28 days of a positive SARS-CoV-2 test and/or COVID-19 recorded as primary or secondary cause of death on the death certificate (using ICD-10 coding).
    Incidence of all-cause mortality in residents
    Incidence of all-cause mortality in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Testing uptake in staff
    Testing uptake in staff, measured as proportion of staff at each home participating in testing during each week of the trial
    Prevalence of SARS-CoV-2 among staff who test
    Prevalence of SARS-CoV-2 among staff who test, measured as proportion of staff with positive test result among those with at least one test recorded during each week of the trial
    Incidence rate of SARS-CoV-2 infections detected in residents
    Incidence rate of SARS-CoV-2 infections detected in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Incidence rate of home-level outbreaks
    Incidence rate of home-level outbreaks, measured as events per 1000 days of follow-up over the duration of the trial
    Duration of outbreaks
    Duration of outbreaks, measured as days from first to last case within outbreaks occurring within the trial period
    Incidence rate of care home closures due to outbreaks
    Incidence rate of care home closures due to outbreaks, measured as events per 1000 days of follow-up over the duration of the trial
    Staff sick
    Proportion of staff per home who are off sick at each home during each week of the trial
    Agency staff filled shifts
    Proportion of all shifts filled by agency staff at each home during each week of the trial

    Full Information

    First Posted
    December 2, 2022
    Last Updated
    December 6, 2022
    Sponsor
    University College, London
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05639205
    Brief Title
    Shaping Care Home COVID-19 Testing Policy
    Acronym
    VIVALDI-CT
    Official Title
    Shaping Care Home COVID-19 Testing Policy: A Pragmatic Cluster Randomised Controlled Trial of Asymptomatic Testing Compared to Standard Care in Care Home Staff.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 2022 (Anticipated)
    Primary Completion Date
    April 2024 (Anticipated)
    Study Completion Date
    April 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University College, London

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The goal of this interventional study is to investigate whether continued use of regular asymptomatic testing in staff is a feasible, effective and cost-effective strategy to reduce the impact of COVID-19 in care homes. The trial aims to quantify the benefits and harms of regular asymptomatic testing in care home staff to inform policy. The rationale for regular asymptomatic testing is that it may reduce the risk of severe disease in residents and the frequency/severity of outbreaks. Participants (care home staff) will perform regular asymptomatic tests for Covid-19. Should they test positive they will be required to refrain from working and be provided with sick pay. Care providers will be reimbursed for the costs of employing agency staff to cover staff sickness absence that results directly from the trial.
    Detailed Description
    To date the evidence based underpinning elements of the intervention has been developed through engagement work with the National Care Forum, senior managers of care homes and three stakeholder events with front-line care home staff. It will be finalised through a series of further workshops. These workshops will 1) consolidate existing insights into routine testing gleaned through past experiences in the COVID-19 pandemic; 2) discuss the intervention prototype; 3) operationalise it in ways which are likely to be acceptable and appropriate within the sector. The testing intervention will comprise of four modules that will be delivered in combination. Module 1: support payments for staff to enable them to self-isolate when unwell. Module 2: Branding and messaging around testing to promote engagement with testing. Module 3: Accessing training, protocols and planning. Module 4: Regular asymptomatic staff testing for COVID-19 using LFDs. Asymptomatic testing will be in addition to symptomatic testing for staff and residents, which is standard policy for all care homes in England. Providers will also receive funding to reimburse costs associated with employing agency staff to cover sickness absence for asymptomatic staff who test positive in the trial. Non-intervention care home residents and staff will be subject to the testing policy that is in place nationally at the time of the trial. Care home staff in control homes will not receive support payments (Module 1) and testing in control homes will not be supported by branding or messaging (Module 2). The degree to which training and testing protocols are already in place in control homes (Module 3) will be investigated in the stakeholder workshops.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COVID-19
    Keywords
    Lateral Flow Device

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    280 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Arm A
    Arm Type
    Active Comparator
    Arm Description
    LFD testing for Covid-19 with sickness support payment. Care providers will receive funding to reimburse the costs of employing agency staff to cover sickness absence in asymptomatic staff who test positive for COVID.
    Arm Title
    Arm B
    Arm Type
    No Intervention
    Arm Description
    Usual Care
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Lateral Flow Device
    Intervention Description
    Regular asymptomatic staff testing with a Lateral Flow Device including support payments if unwell.
    Primary Outcome Measure Information:
    Title
    Primary Outcome
    Description
    The primary outcome is the incidence of COVID-19 related hospital admissions in residents, defined as admissions with a relevant ICD-10 codes (COVID hospitalisations to be defined as any hospital admission record with a primary or secondary ICD10 code of 'U071') and/or admissions in residents who test positive for COVID-19 within 24h following admission or in the 7 days before hospital admission. This has been selected because it is the most important outcome for policymakers.
    Time Frame
    4 months
    Secondary Outcome Measure Information:
    Title
    Incidence rate of hospital admissions
    Description
    Incidence rate of hospital admissions (all-cause) in residents for non-elective care, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Time Frame
    4 months
    Title
    Incidence rate of COVID-associated mortality in residents
    Description
    Incidence rate of COVID-associated mortality in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial. COVID-associated mortality will be defined as death within 28 days of a positive SARS-CoV-2 test and/or COVID-19 recorded as primary or secondary cause of death on the death certificate (using ICD-10 coding).
    Time Frame
    4 months
    Title
    Incidence of all-cause mortality in residents
    Description
    Incidence of all-cause mortality in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Time Frame
    4 months
    Title
    Testing uptake in staff
    Description
    Testing uptake in staff, measured as proportion of staff at each home participating in testing during each week of the trial
    Time Frame
    Once per week for 4 months
    Title
    Prevalence of SARS-CoV-2 among staff who test
    Description
    Prevalence of SARS-CoV-2 among staff who test, measured as proportion of staff with positive test result among those with at least one test recorded during each week of the trial
    Time Frame
    Once per week for 4 months
    Title
    Incidence rate of SARS-CoV-2 infections detected in residents
    Description
    Incidence rate of SARS-CoV-2 infections detected in residents, measured as events per 100,000 person-days of follow-up over the duration of the trial
    Time Frame
    4 months
    Title
    Incidence rate of home-level outbreaks
    Description
    Incidence rate of home-level outbreaks, measured as events per 1000 days of follow-up over the duration of the trial
    Time Frame
    4 months
    Title
    Duration of outbreaks
    Description
    Duration of outbreaks, measured as days from first to last case within outbreaks occurring within the trial period
    Time Frame
    4 months
    Title
    Incidence rate of care home closures due to outbreaks
    Description
    Incidence rate of care home closures due to outbreaks, measured as events per 1000 days of follow-up over the duration of the trial
    Time Frame
    4 months
    Title
    Staff sick
    Description
    Proportion of staff per home who are off sick at each home during each week of the trial
    Time Frame
    Once per week for 4 months
    Title
    Agency staff filled shifts
    Description
    Proportion of all shifts filled by agency staff at each home during each week of the trial
    Time Frame
    Once per week for 4 months

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Only care home staff are eligible to participate in the testing intervention. This includes temporary (agency) staff with no restrictions i.e. catering staff, administrative staff, maintenance staff, in addition to those in a resident-facing role. All care home staff, residents, visitors and relatives are eligible to participate in interviews undertaken as part of the process evaluation. All care home residents at participating home are eligible for data collection and analysis of the outcomes specified. Exclusion Criteria: Visitors, residents and relatives are not eligible to take part in the testing intervention. Staff who visit the care home to provide care but are not employed by the care home e.g. GPs, health visitors are not eligible to take part in either the interviews or the testing intervention.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Laura Shallcross, Professor
    Phone
    0203 549 5540
    Email
    l.shallcross@ucl.ac.uk
    First Name & Middle Initial & Last Name or Official Title & Degree
    CCTU Enquiries
    Phone
    020 7907 4669
    Email
    cctu-enquiries@ucl.ac.uk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Laura Shallcross, Professor
    Organizational Affiliation
    UCL
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    IPD Sharing Plan Description
    The data-sharing plans for the current study are still to be confirmed and will be made available at a later date.

    Learn more about this trial

    Shaping Care Home COVID-19 Testing Policy

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